SILO

GUDID B5211133010

SILO, MIS TUBE

AURORA SPINE, INC.

Sacroiliac joint transarticular fixation/arthrodesis implantation kit

• Primary Device ID: B5211133010
• NIH Device Record Key: 5770702a-effc-481b-92b6-e8e20f70925d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SILO
• Version Model Number: 113-301
• Company DUNS: 079119091
• Company Name: AURORA SPINE, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us
• Phone: 760.424.2004
• Email: info@auroraspine.us

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B5211133010 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

[B5211133010]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-05
• Device Publish Date: 2021-01-28

On-Brand Devices [SILO]

• B5211136000: SILO, INSTRUMENT CASE
• B5211133050: SILO, TAMP
• B5211133040: SILO, DRILL
• B5211133030: SILO, BONE ANCHOR DRIVER
• B5211133020: SILO, BONE ANCHOR
• B5211133010: SILO, MIS TUBE
• B5211133000: SILO, DILATOR
• B52111330810: SiLO Striking Cap